In:
Journal of Applied Polymer Science, Wiley, Vol. 134, No. 1 ( 2017-01-05)
Abstract:
The chemical modification of lignin can greatly enhance its functionality and exploit its application areas. To avoid the difficulties of separation and environmental pollution in the traditional liquid‐phase method, we prepared acetylated lignin by a mechanical‐activation‐assisted solid‐phase synthesis (MASPS) technology with a customized stirring ball mill as a reactor and studied its structure and properties. Ultraviolet–visible analysis showed that the degree of esterification (DE) of the acetylated lignin produced by the MASPS technique was 77.59%, whereas the DEs of those produced by traditional liquid‐phase synthesis (LPS) and thermal solid‐phase synthesis (TSPS) were only 42.29 and 27.54%, respectively. Fourier transform infrared spectroscopy and NMR analyses indicated that both phenolic hydroxyls and aliphatic hydroxyls participated in the reaction, and the reactivity of the phenolic hydroxyls was higher than that of the aliphatic hydroxyl groups. The acetylation of aliphatic hydroxyl mainly happened at the γ of arylglycerol‐β‐aryl ether (β‐O‐4). Scanning electron microscopy analysis showed that the acetylated lignins prepared by MASPS and TSPS were irregular blocks with coarse surfaces and loose structures, whereas the lignin prepared by LPS consisted mostly of regular balls with a smooth surface and a compact structure. Differential scanning calorimetry and thermogravimetric analyses indicated that the glass‐transition temperatures and thermal stability of the acetylated lignin increased by orders with the processing techniques of MASPS, TSPS, and LPS. MASPS integrated the activation and reaction in the same equipment without the use of a solvent and showed advantages of a high efficiency, environmental protection, and easy operation. © 2016 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2016 , 133 , 44276.
Type of Medium:
Online Resource
ISSN:
0021-8995
,
1097-4628
Language:
English
Publisher:
Wiley
Publication Date:
2017
detail.hit.zdb_id:
1491105-X
